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September 3, 2010
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UPCOMING LIVE SEMINARS
Introduction to Clinical Project Management
September 9-10, 2010
Boston, MA
Register
Medical Device GCP Overview
September 13-14, 2010
Philadelphia, PA
Register
Adverse Events: Managing and Reporting for Pharmaceuticals
September 14-15, 2010
Chicago, IL
Register
Comprehensive Monitoring for Medical Devices
October 13-15, 2010
Chicago, IL
Register
Clinical Project Management Advanced
September 20-21, 2010
San Diego, CA
Register
Advanced GCP
September 20-21, 2010
San Diego, CA
Register
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Live Seminars
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Introduction to Clinical Project Management
September 9-10, 2010 | Boston, MA
Medical Device GCP Overview
September 13-14, 2010 | Philadelphia, PA
Adverse Events: Managing and Reporting for Pharmaceuticals
September 14-15, 2010 | Chicago, IL
Monitoring Clinical Drug Studies: Beginner
September 15-17, 2010 | Philadelphia, PA
Advanced GCP
September 20-21, 2010 | San Diego, CA
Clinical Project Management Advanced
September 20-21, 2010 | San Diego, CA
Auditing Techniques for Clinical Research
September 27-28, 2010 | San Diego, CA
Drug Safety and Pharmacovigilance
September 27-28, 2010 | San Diego, CA
Developing Clinical Study Budgets
October 1, 2010 | Philadelphia, PA
Source Documentation
October 1, 2010 | Philadelphia, PA
Clinical Drug Development
October 4-5, 2010 | Philadelphia, PA
The CRA Manager
October 4-5, 2010 | Philadelphia, PA
Data Management in the Electronic Data Capture Arena
October 11-12, 2010 | Philadelphia, PA
Advanced GCP
October 11-12, 2010 | Philadelphia, PA
Conducting Clinical Trials Under ICH GCP
October 11-12, 2010 | Philadelphia, PA
Comprehensive Monitoring for Medical Devices
October 13-15, 2010 | Chicago, IL
Drug Approval Process
October 14-15, 2010 | Philadelphia, PA
Monitoring Clinical Drug Studies: Advanced
October 14-15, 2010 | Philadelphia, PA
Clinical Project Management: Intermediate
October 18-19, 2010 | Boston, MA
Drug Development & FDA Regulations
October 18-19, 2010 | Chicago, IL
Web Seminars
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Final AE Regulatory Guidance
September 3, 2010 | Interactive Web Seminar
Source Documentation: What is Adequate & Accurate?
September 7, 2010 | Interactive Web Seminar
10-Week CRA & CRC: Beginner Program (September 8 - November 10. 2010)
September 8, 2010 | Interactive Web Seminar
Introduction to Data Management
September 9, 2010 | Interactive Web Seminar
Trial Master File (TMF) for Research Sites: Set-Up and Maintenance
September 9, 2010 | Interactive Web Seminar
Special Considerations in Pediatric Trials for CRAs
September 10, 2010 | Interactive Web Seminar
Monitoring Reports: 10 Rules of Effective Report Writing
September 10, 2010 | Interactive Web Seminar
ABCs of Clinical Research for Clinical Administrative Support Staff
September 13, 2010 | Interactive Web Seminar
Essential Documentation in Clinical Trials at Research Sites
September 14, 2010 | Interactive Web Seminar
Monitoring Informed Consent: The Process and Document
September 14, 2010 | Interactive Web Seminar
Meeting International Safety Reporting Requirements
September 15, 2010 | Interactive Web Seminar
Critical Decision Points in Design & Conduct of Patient Registries
September 16, 2010 | Interactive Web Seminar
Clinical Research Site Quality Improvement Strategies
September 17, 2010 | Interactive Web Seminar
Strategies for Managing Difficult Clinical Research Sites
September 17, 2010 | Interactive Web Seminar
How to Prepare and Submit a Bullet Proof 510(k) Submission
September 20, 2010 | Interactive Web Seminar
Adverse Events for Medical Devices
September 21, 2010 | Interactive Web Seminar
Final FDA Guidance for Supervisory Responsibilities of Investigators
September 21, 2010 | Interactive Web Seminar
Facilitation Skills for Clinical Research Professionals
September 21, 2010 | Interactive Web Seminar
Clinical Trial Design for Medical Devices
September 22, 2010 | Interactive Web Seminar
Clinical Trials for Pharmaceuticals: Design and Development
September 23, 2010 | Interactive Web Seminar
Archived Web Seminars
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DVD Train-the-Trainer: Successful Web-Based Training Strategies
July 27, 2010 •
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Single Copy - $795.00
Site License - $1,795.00
DVD Source Documentation: What is Adequate & Accurate?
July 20, 2010 •
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Single Copy - $795.00
Site License - $1,795.00
DVD Meeting HIPAA & FDA Requirements for Case Histories
July 20, 2010 •
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Single Copy - $595.00
Site License - $1,595.00
DVD Monitoring Plan Development
July 19, 2010 •
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Single Copy - $695.00
Site License - $1,695.00
DVD Introduction to Signal Detection and Data Mining
June 28, 2010 •
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DVD Critical Decision Points in Design & Conduct of Patient Registries
June 24, 2010 •
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DVD Study Feasibility: Eliminating Low and Late Enrollment
June 23, 2010 •
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Site License - $1,595.00
DVD Monitoring Phase I Clinical Trials
June 3, 2010 •
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Site License - $1,795.00
DVD Essential Documentation in Clinical Trials at Research Sites
June 1, 2010 •
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Site License - $1,695.00
DVD GCP Training: Core Human Subject Protection Training
May 24, 2010 •
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Single Copy - $595.00
Site License - $1,595.00
DVD Trial Master File (TMF) for Sponsors: Set-Up and Maintenance
May 18, 2010 •
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Single Copy - $795.00
Site License - $1,795.00
DVD Informed Consent Content & Process Requirements
May 13, 2010 •
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Site License - $1,595.00
DVD Fraud in Clinical Research: An Overview
May 12, 2010 •
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Site License - $1,795.00
DVD Site Relationship Management
May 11, 2010 •
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Single Copy - $595.00
Site License - $1,595.00
DVD Monitoring Reports: 10 Rules of Effective Report Writing
May 10, 2010 •
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Single Copy - $795.00
Site License - $1,795.00
DVD Clinical Trial Design for Medical Devices
May 5, 2010 •
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Single Copy - $695.00
Site License - $1,695.00
DVD Adverse Events for Medical Devices
May 4, 2010 •
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Site License - $1,695.00
DVD Corrective Action Plans
April 27, 2010 •
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DVD Electronic Medical Records and Source Document Verification
April 19, 2010 •
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Site License - $1,795.00
DVD Sponsor Management of Investigator Non-Compliance
April 15, 2010 •
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Site License - $1,695.00
Cambridge Healthtech Institute